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Intermediate Clinical Sciences Professional

Description

University of Colorado Anschutz Medical Campus

Department of Pediatrics | Section of Endocrinology

Job Title: Intermediate Clinical Sciences Professional

Position #: 00834516 - Requisition #:36830

Job Summary:

Key Responsibilities:

+ Assist with the day-to-day operations of clinical trials and studies

+ Participate in subject recruitment efforts, including educating potential subjects on the details of the studies through phone contacts, electronic contact, and/or personal interviews, communicating with patients, and all pre-screening/screening activities

+ Obtain the study subject's medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of the subject to participate in a clinical study trial

+ Perform informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required

+ Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy)

+ Collect, code, and analyze data obtained from research in an accurate and timely manner

+ Adhere to research regulatory standards

+ Maintain detailed records of studies to ensure compliance with requirements of the study protocols, department, hospital/clinical standard operating procedures, and/or other regulatory guidelines

+ Ensure that the necessary supplies and equipment for studies are in stock and working order

+ Maintain familiarity with study protocols and documents of assigned research studies.

+ Inventory, handle, and maintain accountability for study supplies and investigational products in collaboration with the laboratory and research pharmacy

+ Perform data and sample collection at in-person and telephone research visits

+ Blood and other specimen handling and processing

+ Enter data and send to the coordinating center

+ Work as a team member in the coordination of assigned primary studies.

+ Participant recruitment, consent, and retention

+ Work with investigators and other staff to prepare IRB submission and maintain study approval and certification

+ Maintain individual certifications needed to perform study duties (e.g., CITI trainings, coordinating center trainings, central and local IRB trainings)

+ Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies

+ Independently perform study-related processes, procedures, and assessments as defined in the study protocol and in compliance with regulating bodies

+ Assist Team Leads, Supervisors, and/or management with the creation and implementation of processes and procedures and quality improvement initiatives

+ Act as a Primary Coordinator on trials/studies

+ Assist and train junior team members

Work Location:

Onsite

Why Join Us:

Why work for the University?

+ Medical: Multiple plan options

+ Dental: Multiple plan options

+ Additional Insurance: Disability, Life, Vision

+ Retirement 401(a) Plan: Employer contributes 10% of your gross pay

+ Paid Time Off: Accruals over the year

+ Vacation Days: 22/year (maximum accrual 352 hours)

+ Sick Days: 15/year (unlimited maximum accrual)

+ Holiday Days: 10/year

+ Tuition Benefit: Employees have access to this benefit on all CU campuses

+ ECO Pass: Reduced rate RTD Bus and light rail service

Qualifications:

Minimum Qualifications:

+ Bachelor's degree in any field

+ One (1) year of clinical research or related experience

+ **Substitution:** A combination of education and related technical/paraprofessional experience may be substituted for the bachelor's degree on a year-for-year basis.

Preferred Qualifications:

+ Bachelor's degree in science or a health-related field

+ Experience with electronic data capture systems (e.g., EMR or EHR and data management systems)

+ Two (2) or more years of clinical research or related experience

+ Fluent in Spanish

+ Experience using REDCap, Epic, OnCore, EndNote, and/or statistical software

+ One (1) or more years of pediatric clinical research experience

+ Experience with diabetes, obesity, and/or human physiology or cardiovascular, and liver research

Knowledge, Skills, and Abilities:

+ Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)

+ Ability to communicate effectively, both in writing and orally

+ Ability to establish and maintain effective working relationships with employees at all levels throughout the institution

+ Outstanding recruiting and customer service skills

+ Ability to multitask to keep track of multiple participants' schedules longitudinally

+ Knowledge of basic human anatomy, physiology, and medical terminology

+ Ability to interpret and master complex research protocol information

+ Ability to handle both blood and laboratory specimens for processing

+ Knowledge of obesity and diabetes physiology

+ Ability to enter data effectively and efficiently

+ Strong interpersonal and communication skills, both in writing and oral

+ Effective organizational and problem-solving skills

+ Accountable and able to take ownership of your tasks and projects

+ Experience with Microsoft Office programs and emails

+ Ability to work independently after the training period

How to Apply:

Screening of Applications Begins:

Anticipated Pay Range:

Equal Employment Opportunity Statement:

ADA Statement:

Background Check Statement:

Vaccination Statement:

Job Category

Primary Location

Schedule

Posting Date

Unposting Date

To apply, visit https://cu.taleo.net/careersection/2/jobdetail.ftl?job=36830&lang=en (https://apptrkr.com/6225086)

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Intermediate Clinical Sciences Professional - 36830 University Staff

A Clinical Sciences Professional is being sought for a full-time position in the Section of Pediatric Endocrinology to work as a study coordinator for clinical research studies dealing with underserved youth with obesity who are at risk for developing type 2 diabetes. The professional research assistant will work with study physicians in endocrinology and pediatrics, midlevel providers, co-investigators and staff both locally and nationally as a part of local studies and a multi-center study and will be responsible for study coordination, participant recruiting, consent, and scheduling, performing study visits, processing of research blood samples and other study samples, placing continuous glucose monitors for home blood sugar monitoring, use of a metabolic cart, exercise testing, institutional review board requirements, tracking of study costs, assisting with MRI and other imaging procedures, entering data and other study-related duties. Travel by car to other sites within Colorado for study recruiting will likely be needed, as may infrequently travel to central study meetings at the NIH in Washington, DC.

- this role is expected to work onsite and is located in Aurora, Colorado.

With an abundance of sunshine and mountains nearby, the Colorado Front Range is the place to be! The University of Colorado Anschutz Medical Campus ranks among the top 20 medical centers in the country. CU Anschutz has top-ranked clinical programs in family medicine and pediatrics, and the basic science and applied health research programs attract more NIH funding than any other university in Colorado. CU-Anschutz is home to the University of Colorado Hospital, The Children's Hospital of Colorado, and the University of Colorado Schools of Medicine, Nursing, Dentistry, Pharmacy and Pharmaceutical Sciences, and Public Health, providing access to an array of possibilities to improve lives across a spectrum of ages and disease states.We have AMAZING benefits and offerexceptional amounts of holiday, vacation, and sick leave! The University of Colorado offers an excellent benefits package, including: There are many additional perks & programs with the CU Advantage (https://apptrkr.com/get\_redirect.php?id=6225086&targetURL=https://advantage.cu.edu/) .

For full consideration, please submit the following document(s):1. A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position 2. Curriculum vitae / Resume3. Three to five professional references, including name, address, phone number (mobile number if appropriate), and email addressQuestions should be directed to: Kristen Nadeau, [email protected] (https://apptrkr.com/get\_redirect.php?id=6225086&targetURL=kristen.nadeau@childrenscolorado.org)

Immediately closes five (5) days after the posting date.

The starting salary range (or hiring range) for this position has been established as $52,721 to$67,061.The above salary range (or hiring range) represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level.Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans, and retirement contributions that add to your bottom line.Total Compensation Calculator: http://www.cu.edu/node/153125 (https://apptrkr.com/get\_redirect.php?id=6225086&targetURL=http://www.cu.edu/node/153125)

The University of Colorado (CU) is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing non-discrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply.

The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at [email protected] (https://apptrkr.com/get\_redirect.php?id=6225086&targetURL=hr.adacoordinator@cuanschutz.edu) .

The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students, and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees.

CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine-preventable diseases (https://apptrkr.com/get\_redirect.php?id=6225086&targetURL=https://www.cdc.gov/vaccines/schedules/downloads/adult/adult-combined-schedule.pdf) . If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety-sensitive job duties, you must enroll in the occupational health medical surveillance program (https://apptrkr.com/get\_redirect.php?id=6225086&targetURL=https://research.cuanschutz.edu/ehs/home/divisions/occupational-health/oh-enrollment) . Application Materials Required: Cover Letter, Resume/CV, List of References : Research Services : Aurora Department: U0001 -- Anschutz Med Campus or Denver - 20971 - SOM-PEDS Endocrinology-GenOps : Full-time : May 12, 2025 : May 18, 2025, 5:59:00 AM Posting Contact Name: Kristen Nadeau Posting Contact Email: [email protected] (https://apptrkr.com/get\_redirect.php?id=6225086&targetURL=kristen.nadeau@childrenscolorado.org) Position Number: 00834516jeid-a4212cc54768834a90f70bcb698ad394

The University of Colorado does not discriminate on the basis of race, color, national origin, sex, age, pregnancy, disability, creed, religion, sexual orientation, gender identity, gender expression, veteran status, political affiliation, or political philosophy. All qualified individuals are encouraged to apply.